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Updated: Jun 28, 2025

A Bioluminescent and Fluorescent Orthotopic Syngeneic Murine Model of Androgen-dependent and Castration-resistant Prostate Cancer
Published on: March 6, 2018
Secondary Cancer after Androgen Deprivation Therapy in Prostate Cancer: A Nationwide Study
Jae Heon Kim1, Gi Hwan Bae2, Jaehun Jung2,3
1Department of Urology, Soonchunhyang University Seoul Hospital, Soonchunhyang University College of Medicine, Seoul, Korea.
Purpose:
Androgen signaling is associated with various secondary cancer, which could be promising for potential treatment using androgen deprivation therapy (ADT). This study investigated whether ADT use was associated with secondary cancers other than prostate cancer in a nationwide population-based cohort.
Materials And Methods:
A total, 278,434 men with newly diagnosed prostate cancer between January 1, 2002 and December 31, 2017 were identified. After applying the exclusion criteria, 170,416 men were enrolled. The study cohort was divided into ADT and non-ADT groups by individual matching followed by propensity score matching (PSM). Study outcomes were incidence of all male cancers. Cox proportional hazard regression models were used to estimate adjusted hazard ratios (HRs) and 95% confidence intervals (CIs) of events.
Results:
During a median follow-up of 4.5 years, a total of 11,059 deaths (6,329 in the ADT group and 4,730 in the non-ADT group) after PSM were found. After PSM, the overall all-cause of secondary cancer incidence risk of the ADT group was higher than that of the non-ADT group (HR: 1.312, 95% CI: 1.23-1.36; adjusted HR: 1.344, 95% CI: 1.29-1.40). The ADT group showed higher risk of overall brain and other central nervous system (CNS) cancer-specific incidence than the non-ADT group (adjusted HR: 1.648, 95% CI: 1.21-2.24). The ADT group showed lower risks of overall cancer-specific incidence for stomach, colon/rectum, liver/inflammatory bowel disease (IBD), gall bladder/extrahepatic bile duct, lung, bladder, and kidney cancers than the non-ADT group. When the duration of ADT was more than 2 years of ADT, the ADT group showed higher risk of cancer-specific incidence for brain and other CNS cancers but lower risk of cancer-specific incidence for liver/IBD and lung cancers than the non-ADT group.
Conclusions:
This study demonstrates that ADT could affect cancer-specific incidence for various cancers.
Insights
Androgen deprivation therapy (ADT) use in prostate cancer patients was linked to a higher risk of secondary cancers, particularly brain and central nervous system (CNS) cancers. However, ADT also showed a reduced risk for several other cancer types.
Area of Science:
- Oncology
- Urology
- Cancer Epidemiology
Background:
- Androgen signaling plays a role in various cancers, making androgen deprivation therapy (ADT) a potential treatment strategy.
- Understanding the association between ADT and secondary cancers is crucial for patient management.
Purpose of the Study:
- To investigate the association between androgen deprivation therapy (ADT) and the incidence of secondary cancers, excluding prostate cancer.
- To analyze cancer-specific incidence rates in a large cohort of men treated for prostate cancer.
Main Methods:
- A nationwide population-based cohort study included 170,416 men diagnosed with prostate cancer between 2002 and 2017.
- Propensity score matching (PSM) was used to create comparable ADT and non-ADT groups.
- Cox proportional hazard regression models analyzed the risk of secondary cancers.
Main Results:
- The ADT group exhibited a higher overall risk of secondary cancer incidence compared to the non-ADT group (adjusted HR: 1.344).
- A significantly increased risk of brain and central nervous system (CNS) cancers was observed in the ADT group (adjusted HR: 1.648).
- The ADT group showed decreased risks for stomach, colon/rectum, liver/IBD, gallbladder, lung, bladder, and kidney cancers.
Conclusions:
- Androgen deprivation therapy (ADT) influences the incidence of various secondary cancers.
- The findings highlight a complex relationship between ADT and secondary cancer risks, with both increased and decreased risks observed for different cancer types.
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